Chapter 16 Flashcards
Describe the phases of the eukaryotic cell cycle
Interphase is further divided into three stages:
- G1 Phase (First Gap): The cell grows physically larger, copies organelles, and makes the molecular building blocks it will need in later steps
- S Phase (Synthesis of DNA): The cell synthesizes a complete copy of the DNA in its nucleus
- G2 Phase (Second Gap): The cell grows more, makes proteins and organelles, and begins to reorganize its contents in preparation for mitosis
Mitotic Phase involves the division of the cell:
1. Mitosis: Nuclear division during which duplicated chromosomes are segregated and distributed into daughter nuclei
2. Cytokinesis: The cell will divide after mitosis in a process where the cytoplasm is divided and two daughter cells are formed
Explain how cyclins and cyclin dependent kinases (cdks) work together to advance a cell through the eukaryotic cell cycle
Cyclins are a group of related proteins that are associated with specific phases or transitions in the cell cycle and help drive the events of that phase. The levels of different cyclins vary across the cell cycle. A typical cyclin is present at low levels for most of the cycle, but increases strongly at the stage where it’s needed
Cyclin-dependent kinases (Cdks) are a family of enzymes that regulate cell cycle progression in combination with cyclins. A lone Cdk is inactive, but the binding of a cyclin activates it, making it a functional enzyme and allowing it to modify target proteins
Here’s how they work together:
1. Activation: Cyclins are synthesized and bind to Cdks, forming a cyclin-Cdk complex. This complex acts as a signal to the cell to pass to the next cell cycle phase
- Regulation: The cyclin-Cdk complex modifies target proteins inside the cell. Cdks are kinases, enzymes that phosphorylate (attach phosphate groups to) specific target proteins. The attached phosphate group acts like a switch, making the target protein more or less active
- Deactivation: Eventually, the cyclin degrades, deactivating the Cdk, thus signaling exit from a particular phase
Discuss the events that occur during each of the cell cycle checkpoints
These checkpoints monitor the order, integrity, and fidelity of the major events of the cell cycle. These checkpoints ensure that cells don’t divide under unfavorable conditions, such as when their DNA is damaged, or when there isn’t room for more cells in a tissue or organ2. They are crucial for maintaining the health and functionality of cells. There’s three of them:
1. G1 Checkpoint (G1/S transition): This is the main decision point for a cell, the primary point at which it must choose whether or not to divide. Here, a cell checks whether internal and external conditions are right for division. Factors assessed include cell size, nutrient availability, molecular signals, and DNA integrity. If a cell doesn’t get the go-ahead cues it needs at the G1 checkpoint, it may leave the cell cycle and enter a resting state called G0 phase
- G2 Checkpoint (G2/M transition): This checkpoint ensures all of the chromosomes have been accurately replicated and that the replicated chromosome is not damaged before the cell enters mitosis. It acts as an additional checkpoint before M phase to make sure that cell division goes smoothly
- M Checkpoint (Spindle Checkpoint): This checkpoint occurs at the end of the metaphase of mitosis. It ensures that all chromosomes are properly attached to the spindle microtubules, allowing for equal distribution of chromosomes during cell division
Describe how the replication of eukaryotic chromosomes produces sister chromatids
The replication of eukaryotic chromosomes occurs during the S phase (synthesis phase) of the cell cycle. Here’s how it produces sister chromatids:
- DNA Replication: During the S phase, each chromosome is replicated to produce two identical copies. This process involves unwinding the DNA double helix and using each strand as a template to synthesize a new complementary strand
- Formation of Sister Chromatids: The result of this replication is two identical DNA molecules, which are called sister chromatids. These sister chromatids are held together at a region called the centromere
- Cohesion: Cohesin proteins hold the sister chromatids together at the centromere, ensuring they stay attached until they are separated during cell division
So, in essence, the replication of eukaryotic chromosomes during the S phase results in the formation of sister chromatids, which are two identical copies of the original chromosome
Explain the structure and function of the mitotic spindle
Structure:
- The mitotic spindle is made of long fibers called microtubules. Hundreds or even thousands of these microtubules form the mitotic spindle
- Microtubules are rope-like components of the cytoskeleton. They act as a rope that lengthens and shortens to move duplicated chromosomes from the parent cell into the daughter cells
- The spindle apparatus is vaguely ellipsoid in cross section and tapers at the ends. In the wide middle portion, known as the spindle midzone, antiparallel microtubules are bundled by kinesins
- At the pointed ends, known as spindle poles, microtubules are nucleated by the centrosomes in most animal cells
Function:
- The mitotic spindle is necessary to equally divide the chromosomes in a parental cell into two daughter cells during both types of nuclear division: mitosis and meiosis
- During interphase, which occurs before mitosis, a parent cell’s chromosomes and DNA are replicated. During prophase, the mitotic spindle forms
- The duplicated chromosomes have a narrow midsection, called the centromere, which is the attachment point of the two chromosomes. Some of these attach to the central region of the sister chromatids, called the kinetochore
- The dynamic lengthening and shortening of spindle microtubules, through a process known as dynamic instability, determines to a large extent the shape of the mitotic spindle and promotes the proper alignment of chromosomes at the spindle midzone
- Once every chromosome is bi-oriented, anaphase commences and cohesin, which couples sister chromatids, is severed, permitting the transit of the sister chromatids to opposite poles
Outline the key events that occur during the phases of mitosis
Mitosis is a type of cell division that results in two daughter cells each having the same number and kind of chromosomes as the parent nucleus. It consists of four basic phases:
- Prophase: The chromatin condenses into discrete chromosomes. The nuclear envelope breaks down and spindles form at opposite poles of the cell. Chromatin fibers become coiled into chromosomes, with each chromosome having two chromatids joined at a centromere. The mitotic spindle, composed of microtubules and proteins, forms in the cytoplasm
- Metaphase: The spindle reaches maturity and the chromosomes align at the metaphase plate, a plane that is equally distant from the two spindle poles. Chromosomes move randomly until they attach (at their kinetochores) to polar fibers from both sides of their centromeres
- Anaphase: Chromatids break apart at the centromere and move to opposite poles. This is facilitated by the shortening of the microtubules
- Telophase: Two nuclei are formed after nuclear envelopes reform around each group of chromosomes. The chromosomes begin to decondense, returning to their stringy form
Describe the processes of synapsis and crossing over
Synapsis: This is the fusion of chromosome pairs at the start of meiosis. It mainly occurs during prophase I of meiosis I. A protein complex called the synaptonemal complex connects the homologues. The genes on the chromatids of the homologous chromosomes are aligned precisely with each other. The tight pairing of the homologous chromosomes is called synapsis. This helps to ensure that each cell divides a full set of chromosomes.
Crossing Over: This is the exchange of genetic material between homologous chromosomes after the tetrad forms. When synapsis happens, the homologous chromosomes end up next to each other. One of the sister chromatids from each chromosome will have the chance to exchange genetic material with a sister chromatid from the homologous chromosome. The points where homologs crossover and exchange genetic material are known as a chiasmata. These are chosen more or less at random, and they will be different in each cell that goes through meiosis. This repetition produces a wide variety of recombinant chromosomes, chromosomes where fragments of DNA exchanged between homologs
Outline the key events that occur during the phases of meiosis
Meiosis is a type of cell division that results in four daughter cells each with half the number of chromosomes of the parent cell. It consists of two rounds of division, meiosis I and meiosis II, and each round has four stages: prophase, metaphase, anaphase, and telophase
Meiosis I:
Prophase I: Chromosomes condense and homologous chromosomes pair up. The nuclear envelope breaks down and spindles form. Crossing over, the exchange of genetic material between homologous chromosomes, occurs
Metaphase I: Homologous pairs of chromosomes align at the metaphase plate.
Anaphase I: Homologous pairs separate and move to opposite poles.
Telophase I: Two new cells form, each with a haploid number of chromosomes.
Meiosis II:
Prophase II: The nuclear envelope breaks down and new spindles form.
Metaphase II: Chromosomes align at the metaphase plate.
Anaphase II: Sister chromatids separate and move to opposite poles.
Telophase II: Four new haploid cells form
Compare and contrast mitosis and meiosis
Mitosis:
Purpose: Mitosis is how new body cells are produced for growth and repair
Divisions: It involves one round of cell division
Daughter Cells: Produces two daughter cells
Chromosome Number: The daughter cells are diploid (2n), meaning they have the same number of chromosomes as the parent cell
Genetic Variation: The daughter cells are genetically identical to the parent cell
Crossing Over: No crossing-over occurs
Meiosis:
Purpose: Meiosis is used to produce gametes (i.e., sperm and egg cells) for sexual reproduction
Divisions: It involves two rounds of cell division
Daughter Cells: Produces four daughter cells
Chromosome Number: The daughter cells are haploid (n), meaning they have half the number of chromosomes as the parent cell
Genetic Variation: The daughter cells are genetically unique due to crossing over and independent assortment
Describe an advantage of sexual reproduction
Genetic Diversity: Sexual reproduction creates genetic variation in the offspring. This diversity is due to the combination of genetic material from two parents, which results in offspring that are genetically unique
Adaptation: The genetic variation produced by sexual reproduction allows species to adapt to new environments. This gives them a survival advantage as they can evolve and cope with environmental changes
Disease Resistance: A greater level of genetic diversity allows for higher levels of natural disease resistance within a species. This is because pathogens are unable to adapt to one specific genetic profile
Evolutionary Advancements: Genetic variation can lead to evolutionary advancements. This is similar to the “survival of the fittest” principles that Charles Darwin first introduced
Distinguish among the life cycles of diploid-dominant species, haploid-dominant species, and species that exhibit an alternation of generations
Diploid-Dominant Life Cycle: In this type of life cycle, the multicellular diploid stage is the most obvious life stage. Nearly all animals, including humans, employ a diploid-dominant life cycle strategy where the only haploid cells produced by the organism are the gametes. Early in the development of the embryo, specialized diploid cells, called germ cells, are produced within the gonads. Germ cells are capable of mitosis to perpetuate the cell line and meiosis to produce gametes. Once the haploid gametes are formed, they lose the ability to divide again. There is no multicellular haploid life stage
Haploid-Dominant Life Cycle: In this type of life cycle, the multicellular haploid stage is the most obvious life stage. All fungi and some algae have a haploid-dominant life cycle. The single-celled zygote is the only diploid cell. In this type of life cycle, the multicellular (or sometimes unicellular) haploid stage is often multicellular
Alternation of Generations: In this type of life cycle, both the haploid and the diploid stages are multicellular. This is seen in plants and some algae. Both the haploid and the diploid stages are apparent to different degrees depending on the group
Binary Fission
Binary fission is a relatively simple process, compared to mitosis, because binary fission does not involve reproducing organelles or complex chromosomes. It’s the process that bacteria use to carry out cell division. It’s actually how bacteria reproduce, or add more bacteria to the population
Binary fission is a type of asexual reproduction where a parent cell divides, resulting in two identical cells, each having the potential to grow to the size of the original cell. It’s the process through which asexual reproduction happens in bacteria. Here’s how it works:
- DNA Replication: The process starts with the replication of the DNA within the cell. Mitochondria must also replicate their DNA before binary fission, though other organelles have no DNA
- Separation of DNA: Then, the DNA is separated into alternate ends of the single cell
- Cell Division: The plasma membrane pinches the cell apart, and one cell becomes two. With a fully-functioning DNA molecule, each cell is then capable of all the functions of life
- Formation of Independent Organisms: Therefore, the cells become independent organisms. Organelles, though they are not independent organisms, separate in this way as well
M-phase
The M-phase, also known as the mitotic phase, is a stage in the cell cycle where cell division takes place. It is composed of two distinct processes: mitosis and cytokinesis
Mitosis is a form of asexual cell reproduction in eukaryotes, equivalent in most respects to binary fission in prokaryotes. It includes prophase, prometaphase, metaphase, anaphase, and telophase, and it relies on the mitotic spindle at each cell pole
Cytokinesis is the process where the cell divides its cytoplasm to make two new cells
During the M-phase, the cell divides its copied DNA and cytoplasm to make two new, identical daughter cells. The M-phase is the most busy and dramatic part of the cell cycle, but the cell actually spends most of its time in interphase. The end of the G2 phase is signaled by a protein, marking what is called a G2 checkpoint. A similar G2 checkpoint marks the start of the M phase
Interphase
Interphase is the phase of the cell cycle in which a typical cell spends most of its life. It is the longest stage in the eukaryote cell cycle. During interphase, the cell acquires nutrients, creates and uses proteins and other molecules, and starts the process of cell division by replicating the DNA
- Gap 1 (G1): The cell performs its normal functions, and grows in size. The cell replicates organelles as necessary
- Synthesis (S): During synthesis, the cell pauses its normal functioning. All resources are dedicated to replicating the DNA. This process starts with the two entwined stands of DNA being “unzipped” by various proteins. Other proteins, known as polymerase enzymes, start creating new strands to pair with each half of the DNA
- Gap 2 (G2): The cell synthesizes proteins and continues to increase in size
The purpose of interphase in all cell types is to prepare for cell division, which happens in a different stage of the cell cycle. Depending on which species of organism is dividing, the functions of the cell during interphase can vary widely
G0,G1,S,G2,M
- G0 Phase: Cells in the G0 phase are not actively preparing to divide. The cell is in a quiescent (inactive) stage that occurs when cells exit the cell cycle
- G1 Phase (First Gap): During G1 phase, the cell grows physically larger, copies organelles, and makes the molecular building blocks it will need in later steps
- S Phase (Synthesis of DNA): In S phase, the cell synthesizes a complete copy of the DNA in its nucleus
- G2 Phase (Second Gap): During the second gap phase, or G2 phase, the cell grows more, makes proteins and organelles, and begins to reorganize its contents in preparation for mitosis
- M Phase (Mitotic Phase): During the mitotic (M) phase, the cell separates its DNA into two sets and divides its cytoplasm, forming two new cells
These phases occur in strict sequential order, and cytokinesis - the process of dividing the cell contents to make two new cells - starts in anaphase or telophase. The goal of the cell cycle is to ensure that each daughter cell gets a perfect, full set of chromosomes
DNA Polymerase
DNA Polymerase plays a crucial role in both mitosis and meiosis, as it is responsible for replicating the DNA in a cell before it divides
Mitosis: During the interphase of the mitotic cell cycle, specifically in the S phase, DNA Polymerase helps in duplicating the cell’s DNA. This replication is necessary so that when the cell divides during mitosis, each new daughter cell will have a complete set of DNA
Meiosis: Similar to mitosis, DNA Polymerase also plays a key role in the DNA replication that occurs during the S phase of meiosis. This replication results in the formation of sister chromatids, which are then separated during the two divisions of meiosis. This ensures that the resulting gametes have the correct number of chromosomes
In both processes, DNA Polymerase adds nucleotides to the 3’ end of the template, synthesizing a new strand of DNA that is complementary to the template strand. This enzyme is essential for the accurate replication of the genome and thus for the production of new cells in both mitosis and meiosis
Histones
Histones are highly basic proteins found in eukaryotic cell nuclei and in most Archaeal phyla. They act as spools around which DNA winds to create structural units called nucleosomes. Nucleosomes in turn are wrapped into 30-nanometer fibers that form tightly packed chromatin
The tight wrapping of DNA around histones is largely due to the electrostatic attraction between the positively charged histones and the negatively charged phosphate backbone of DNA
Histones play important roles in gene regulation and DNA replication. They can be chemically modified through the action of enzymes to regulate gene transcription. The most common modifications are the methylation of arginine or lysine residues or the acetylation of lysine. Methylation can affect how other proteins such as transcription factors interact with the nucleosomes. Lysine acetylation eliminates a positive charge on lysine, thereby weakening the electrostatic attraction between histone and DNA, resulting in partial unwinding of the DNA, making it more accessible for gene expression
Chromatid vs. Sister Chromatid
In summary, a chromatid refers to one half of a duplicated chromosome, while sister chromatids refer to the paired identical copies of a chromosome
A chromatid is one of two strands of a copied chromosome. When a chromosome is replicated, it splits longitudinally, creating two identical copies. These copies are called chromatids
Sister chromatids are two identical copies of the same chromosome formed by DNA replication, attached to each other by a structure called the centromere. During cell division, they are separated from each other, and each daughter cell receives one copy of the chromosome. Sister chromatids are formed in both the cellular division processes of mitosis and meiosis
Homolog/Homologous
In biology, a homolog refers to a structure, sequence, gene, or chromosome that is similar in different organisms, usually indicating a common ancestry. Homologs can be proteins, DNA sequences, or anatomical structures. Homology between protein or DNA sequences is defined in terms of shared ancestry
Homologous is an adjective form of the term “homolog”. It describes traits, structures, or sequences that are similar because of shared ancestry. For example, the forelimbs of humans and the wings of bats are homologous structures. They may serve different functions, but they share a common ancestral origin
In genetics, the term “homolog” is used both to refer to a homologous protein and to the gene (DNA sequence) encoding it. Homologous sequences are also called conserved. This is not to be confused with conservation in amino acid sequences in which the amino acid at a specific position has been substituted with a different one with functionally equivalent physicochemical properties. One can, however, refer to partial homology where a fraction of the sequences compared (are presumed to) share descent, while the rest does not. For example, partial homology may result from a gene fusion event
Chromosome
A chromosome is a long DNA molecule with part or all of the genetic material of an organism. In most chromosomes, the very long thin DNA fibers are coated with packaging proteins; in eukaryotic cells, the most important of these proteins are the histones. These proteins, aided by chaperone proteins, bind to and condense the DNA molecule to maintain its integrity
Chromosomes are normally visible under a light microscope only during the metaphase of cell division (where all chromosomes are aligned in the center of the cell in their condensed form). Before this happens, each chromosome is duplicated (S phase), and both copies are joined by a centromere, resulting either in an X-shaped structure (pictured above), if the centromere is located equatorially, or a two-arm structure, if the centromere is located distally. The joined copies are now called sister chromatids
Chromosomes play a significant role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe. Usually, this will make the cell initiate apoptosis leading to its own death, but sometimes mutations in the cell hamper this process and thus cause progression of cancer. Some use the term chromosome in a wider sense, to refer to the individualized portions of chromatin in cells, either visible or not under light microscopy
Centrosome vs Centromere
Centrosome: A centrosome is an organelle made up of microtubules. It nucleates all the microtubules inside a cell to form the spindle apparatus during the prophase of cell division. Centrosomes are only found in animal cells, where they organize the microtubules and monitor the cell cycle. The centrosome is usually attached to the plasma membrane. During the prophase of the cell division, the centrosome duplicates to form two centrosomes, and these two centrosomes move to the opposite poles of the cell
Centromere: A centromere is a highly constricted region of DNA found in the middle of the chromosome. It holds the two sister chromatids together during cell division. The prime activity of the centromere is to provide a location in the center of a chromosome for microtubule binding through kinetochores. Centromeres occur in all eukaryotic cells and are responsible for the movement of chromosomes at the time of mitosis.
In summary, a centrosome is an organelle that organizes microtubules and forms the spindle apparatus for cell division, while a centromere is a region of DNA that holds sister chromatids together during cell division
Kinetochore
A kinetochore is a disc-shaped protein structure associated with duplicated chromatids in eukaryotic cells. It’s where the spindle fibers attach during cell division to pull sister chromatids apart. The kinetochore assembles on the centromere and links the chromosome to microtubule polymers from the mitotic spindle during mitosis and meiosis
The kinetochore contains two regions: an inner kinetochore, which is tightly associated with the centromere DNA and assembled in a specialized form of chromatin that persists throughout the cell cycle; and an outer kinetochore, which interacts with microtubules. The outer kinetochore is a very dynamic structure with many identical components, which are assembled and functional only during cell division
Kinetochores start, control, and supervise the striking movements of chromosomes during cell division. During mitosis, two sister chromatids are held together by a centromere. Each chromatid has its own kinetochore, which face in opposite directions and attach to opposite poles of the mitotic spindle apparatus. Following the transition from metaphase to anaphase, the sister chromatids separate from each other, and the individual kinetochores on each chromatid drive their movement to the spindle poles that will define the two new daughter cells
Microtubule
Microtubules play a crucial role in both mitosis and meiosis, as they are involved in the separation and movement of chromosomes during these processes
Mitosis: During mitosis, microtubules form the mitotic spindle, a structure that separates replicated chromosomes to opposite sides, creating two daughter cells. The choreography of microtubules, centrosomes, and chromosomes during mitosis is beautifully designed by nature. Finely regulated and synchronized movements of these super-macromolecular complexes against the entropic forces within a dividing cell ensure the fidelity of the genetic material in both daughter cells
Meiosis: Similar to mitosis, microtubules also play a key role in meiosis. They contribute to the formation of the meiotic spindle, which is used to pull apart homologous chromosomes during meiosis I and sister chromatids during meiosis II
In both processes, microtubules, as part of the spindle apparatus, attach to the chromosomes at the kinetochores, which are protein structures located at the centromeres. This attachment allows the microtubules to move the chromosomes to the correct locations during cell division
Spindle Fiber
Spindle fibers are aggregates of microtubules that move chromosomes during cell division. They are found in eukaryotic cells and are a component of the cytoskeleton. The spindle apparatus of a cell, which includes spindle fibers, motor proteins, chromosomes, and in some animal cells, microtubule arrays called asters, ensures even chromosome distribution between daughter cells during mitosis and meiosis
In mitosis, spindle fibers are highly active. They migrate throughout the cell and direct chromosomes to go where they need to go. The process involves several stages:
Prophase: Spindle fibers form at opposite poles of the cell
Metaphase: Spindle fibers called polar fibers extend from cell poles toward the midpoint of the cell known as the metaphase plate
Anaphase: Spindle fibers pull apart the sister chromatids to opposite poles of the cell
In meiosis, spindle fibers function similarly, where four daughter cells are formed instead of two, by pulling homologous chromosomes apart after they have been duplicated to prepare for division
Karyotype
A karyotype is the complete set of chromosomes of an individua. It describes the chromosome count of an organism and what these chromosomes look like under a light microscope. Attention is paid to their length, the position of the centromeres, banding pattern, any differences between the sex chromosomes, and any other physical characteristics
In both mitosis and meiosis, karyotypes can be used to identify the chromosome number and any abnormalities. During these processes, cells are often arrested during metaphase when chromosomes are most condensed. Metaphase chromosomes are then photographed, and a karyotype is produced
In mitosis, which occurs outside of the reproductive organs, a normal diploid organism will have autosomal chromosomes present in two copies. For example, a diploid human nucleus has 23 pairs of chromosomes (2n=46)
In meiosis, which occurs in the reproductive organs, the chromosome number in the germ-line (the sex cells) is n (humans: n = 23). This process leads to the formation of four daughter cells, each with a haploid set of chromosomes
Overall, karyotyping is a powerful tool in cytogenetics, allowing for the detection of chromosomal abnormalities and providing valuable information about cellular function and past evolutionary events
Prophase and Prometaphase
In prophase:
- The chromosomes condense and become visible
- The nuclear envelope remains intact
- The centrosomes, which are the organizing centers of microtubules, begin to separate towards opposite poles of the cell
- The mitotic spindle, an arrangement of microtubules responsible for aligning duplicated chromosomes in later phases, begins to form
In prometaphase:
- The nuclear envelope breaks down, releasing the chromosomes
- The mitotic spindle grows more, and some of the microtubules start to capture chromosomes
- The kinetochores, which are the attachment points for the spindle microtubules, become fully matured on the centromeres of the chromosomes
- The disruption of the nuclear envelope allows for the mitotic spindles to gain access to the mature kinetochores
- Once they have captured chromosomes, the kinetochore microtubules begin to exert force on the chromosomes, moving them
Metaphase
In metaphase:
- The chromosomes align along the spindle’s center
- A spindle assembly checkpoint occurs during metaphase in both mitosis and meiosis. If these checkpoints are skipped, or do not function properly, the cell will begin anaphase before the chromosomes are properly attached to microtubules and aligned on the metaphase plate
In anaphase:
- The phase separates duplicate genetic materials that are carried in the nucleus of the parent cell, into two identical daughter cells
- During anaphase, each pair of chromosomes separates into two identical but independent chromosomes
- Separation occurs simultaneously at the centromere and each separated chromosome gets pulled by the spindles to the opposite poles of the cell
- The function of anaphase is to ensure that each daughter cell receives identical sets of chromosomes before the final phase of the cell cycle, which is telophase
Telophase and Cytokinesis
In telophase:
- The nuclear envelopes reform around the new nuclei in each half of the dividing cell
- The nucleolus, or ribosome producing portions of the nucleus return
- The chromosomes release from their tightly bound structure back into loose chromatin
- The main parts of the spindle apparatus fall apart
Cytokinesis is the process in which the cell actually divides into two. With the two nuclei already at opposite poles of the cell, the cell cytoplasm separates, and the cell pinches in the middle, ultimately leading to cleavage. The first signs of this puckering are usually visible sometime during anaphase. The disassembled cytoskeletal filaments are used in a different way during cytokinesis. Cleavage occurs by the contraction of a thin ring of actin filaments that form the contractile ring. The contractile ring defines the cleavage line for the cell. If the ring is not positioned at the center of the cell, an asymmetrical division takes place. The ring contracts and eventually pinches the cell until it separates into two independent daughter cells